v1
Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria.
Identifier:nobleid.org/w1/20260515/F3593CDA
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/F3593CDA)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims